Ireland
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Enrolling by invitation Observational

Safety, Feasibility, and Acceptability of the MINERVA Voice Conversational Agent for Emergency Department History-Taking

NCT07877883 · tracked via the Priya Life Science Israel tracker
Phase
Observational
Started
2026-10-01
Last updated
2026-10-16

Condition(s) studied

History TakingArtificial Intelligence (AI)

Investigational drug(s) / intervention(s)

MINERVA AI Chatbot

MINERVA AI Chatbot: The MINERVA AI chatbot is AI software that allows patients to provide medical history through text or voice.

Study summary

This study evaluates whether an artificial intelligence (AI) conversational agent called MINERVA (Medical Interface for Navigating the Emergency Room with Voice Assistance) can safely and feasibly gather medical histories from emergency department (ED) patients and produce accurate summaries. The main questions it aims to answer are:

Can an AI conversational agent gather and summarize patient histories in the emergency department?

Are the resulting summaries accurate? Do they capture essential clinical information?

Can an AI agent overseeing these conversations independently identify red-flag symptoms that may need time-sensitive clinical interventions?

Adult ED patients interact with MINERVA via either voice chat or typing on a keyboard. MINERVA asks them questions about their symptoms and generates a summary which the patients review for accuracy. MINERVA reviews the conversation for clinical red flags that suggest urgent evaluation is required. Participants fill out a survey providing feedback on their experience. The summary is not saved in the medical record and clinical care is not affected.

Physician reviewers will evaluate the safety, accuracy, and clinical value of the MINERVA interview transcripts and summaries using standardized rubrics, including whether MINERVA was correct in identifying red-flag symptoms that may need time-sensitive clinical interventions.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients aged ≥18 years. * Patient underwent triage in the ED. * English-speaking. Exclusion Criteria: * Critical illness precluding interaction with MINERVA. * Inability to provide consent. * Significant hearing/speech/typing impairments precluding interaction by text or voice. * Prisoners. * Inability to follow study procedures. * Patients requiring isolation precautions incompatible with study procedures.

Primary outcome measure(s)

  • Safety Diagnoses — 1 Day
    Emergency physicians will review each patient-AI interview transcript using a standardized rubric to determine whether evaluation for possible myocardial infarction, acute stroke, or sepsis is warranted. MINERVA's assessments will be compared with these physician assessments.

Trial sites (1)

FacilityCityRegionStatus
Beth Israel Deaconess Medical Center Boston Massachusetts
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07877883 on ClinicalTrials.gov ↗ ← All trials in Israel